The unseen third dimension: a novel approach for assessing head shape severity in infants with isolated sagittal synostosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00381-019-04246-5.pdf
Reference19 articles.
1. Chummun S, McLean NR, Flapper WJ, David DJ (2016) The management of nonsyndromic, isolated sagittal synostosis. J Craniofac Surg 27(2):299–304. https://doi.org/10.1097/SCS.0000000000002363
2. Hunter AG, Rudd NL (1976) Craniosynostosis. I. Sagittal synostosis: its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s). Teratology 14(2):185–193. https://doi.org/10.1002/tera.1420140209
3. Wilkie AO, Wall SA (1996) Craniosynostosis: novel insights into pathogenesis and treatment. Curr Opin Neurol 9(2):146–152
4. Fearon JA, McLaughlin EB, Kolar JC (2006) Sagittal craniosynostosis: surgical outcomes and long-term growth. Plast Reconstr Surg 117(2):532–541. https://doi.org/10.1097/01.prs.0000200774.31311.09
5. Schmelzer RE, Perlyn CA, Kane AA, Pilgram TK, Govier D, Marsh JL (2007) Identifying reproducible patterns of calvarial dysmorphology in nonsyndromic sagittal craniosynostosis may affect operative intervention and outcomes assessment. Plast Reconstr Surg 119(5):1546–1552. https://doi.org/10.1097/01.prs.0000256067.42651.30
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